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Associate Director, Quality Management

Job in Columbus, Platte County, Nebraska, 68602, USA
Listing for: BD
Full Time position
Listed on 2025-12-27
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
Job Description & How to Apply Below

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Job Description Summary

BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of Med Tech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.

We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Become a maker of possible with us.

We are seeking a dynamic and experienced Associate Director, Quality Management to drive organizational change and grow within our company. This pivotal leadership role will ensure site quality and compliance procedures align with BD standards, regulatory requirements, and customer specifications while fostering a culture of continuous improvement. The role ensures compliance with BD quality systems, policies, procedures and best practices, and all local, state, federal and BD safety regulations, policies and procedures.

Regular, punctual attendance is an essential job function. Ability to read and write and converse in English. Willing and able to uphold BD Values.

About

The Role

As the Site Quality Leader, you will oversee multiple quality functions including Quality Assurance, Quality Control, Quality Systems & Compliance, and Quality Engineering for Pharmaceutical Systems and BDX Molding Center of Excellence. Reporting to the Senior Director of Quality Operations, you’ll serve as a key member of the site leadership team while contributing to worldwide functional strategy and priorities.

Key Responsibilities
  • Strategic Leadership:
    Develop and maintain comprehensive plant quality and compliance strategies, policies, and frameworks that drive organizational excellence and regulatory adherence.
  • Team Development:
    Lead, coach, and develop a high‑performing quality team, fostering professional growth while building a cohesive department that maintains strong quality presence across manufacturing areas.
  • Regulatory Interface:
    Serve as the plant "management representative" for notified bodies, regulatory authorities, and customers, managing audits and ensuring effective resolution of findings.
  • Cross-Functional Collaboration:

    Build influential networks with worldwide Quality and Regulatory functions, other plant Quality Leaders, and key global functions (R&D, Engineering, Supply Chain) to ensure alignment around priorities.
  • Quality Systems Management:
    Direct operational leadership in planning and managing comprehensive quality systems including:
    • Validation programs
    • Internal and customer quality audits
    • Compliance audits
    • Corrective and preventive action programs (CAPA)
    • GMP training initiatives
    • Quality engineering
    • Change control processes
    • Document control systems
    • Complaint management
  • Continuous Improvement:
    Identify quality improvement opportunities within operations and partner with peers in Manufacturing, Engineering, and Supply Chain to develop and implement innovative solutions.
  • Resource Management:
    Ensure the quality organization is properly staffed, organized, and resourced to fulfill cGMP obligations and BD procedures.
  • Cultural Transformation:
    Champion and promote a culture of quality excellence throughout the plant, driving organizational change that elevates quality standards.
Qualifications Education
  • Required:

    Bachelor's degree in a technical or science‑related field
  • Preferred:
    Advanced degree in a technical or science‑related discipline
Experience
  • 10+ years of experience in pharmaceutical/biopharmaceutical manufacturing environments (highly preferred)
  • 10+ years in plant Quality leadership roles with demonstrated success (highly preferred)
  • Comprehensive knowledge of 21

    CFR parts 820 (QSR), 210/211, ISO
    9001, 13485 with experience leading or participating in related audits and inspections
  • Experience in production or engineering management (preferred)
  • Mul…
Position Requirements
10+ Years work experience
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